434 research outputs found

    Nonperturbative renormalization in classical φ4 theory

    Get PDF
    This is an in-depth study of two analytic nonperturbative renormalization group methods used to study nonrelativistic quartic interacting systems. The model studied is that of classical real scalar φ4 theory. A variety of techniques are used including a rescaling of a nonlinear complete basis, a limit of finite periodic systems, and an analytic calculation of RG equations using a limit of finite systems. Assuming that the truncated forms of the action employed do not change the physics and that standard scaling techniques can be transcribed from more conventional RG approaches to these truncated forms, key results are a new fixed point at strong coupling with exponents ν=2/d and η=2 - d/2 as well as a nonperturbative generation of RG equations and subsequent solution to reduced φ4 theory. A nontrivial critical point for d=3 is identified in this reduced model with ν=4/(1+√41) ≈ 0.540 and η=0

    Material Availability: A Study of Academic Library Performance

    Get PDF
    This article reports the findings of a study modeled after Saracevic, Shaw, and Kantor\u27s efforts to identify and quantify the causes of users\u27 failures to identify and locate library materials. The researchers analyzed patron-reported and librarian-observed subject and known-item searches and found an overall success rate of only 54 percent. The problems that led to the 46 percent failure rate were analyzed by source and type of failure, and subjective observations concerning problems encountered by patrons were recorded. Recommendations are made for reducing library malfunctions and circulation, patron, and acquisition errors

    Uncertainty propagation for flood forecasting in the Alps: different views and impacts from MAP D-PHASE

    Get PDF
    D-PHASE was a Forecast Demonstration Project of theWorldWeather Research Programme (WWRP) related to the Mesoscale Alpine Programme (MAP). Its goal was to demonstrate the reliability and quality of operational forecasting of orographically influenced (determined) precipitation in the Alps and its consequences on the distribution of run-off characteristics. A special focus was, of course, on heavy-precipitation events. The D-PHASE Operations Period (DOP) ran from June to November 2007, during which an end-to-end forecasting system was operated covering many individual catchments in the Alps, with their water authorities, civil protection organizations or other end users. The forecasting system’s core piece was a Visualization Platform where precipitation and flood warnings from some 30 atmospheric and 7 hydrological models (both deterministic and probabilistic) and corresponding model fields were displayed in uniform and comparable formats. Also, meteograms, nowcasting information and end user communication was made available to all the forecasters, users and end users. D-PHASE information was assessed and used by some 50 different groups ranging from atmospheric forecasters to civil protection authorities or water management bodies. In the present contribution, D-PHASE is briefly presented along with its outstanding scientific results and, in particular, the lessons learnt with respect to uncertainty propagation. A focus is thereby on the transfer of ensemble prediction information into the hydrological community and its use with respect to other aspects of societal impact. Objective verification of forecast quality is contrasted to subjective quality assessments during the project (end user workshops, questionnaires) and some general conclusions concerning forecast demonstration projects are drawn

    Sources of light-absorbing aerosol in arctic snow and their seasonal variation

    Get PDF
    Two data sets consisting of measurements of light absorbing aerosols (LAA) in arctic snow together with suites of other corresponding chemical constituents are presented; the first from Siberia, Greenland and near the North Pole obtained in 2008, and the second from the Canadian arctic obtained in 2009. A preliminary differentiation of the LAA into black carbon (BC) and non-BC LAA is done. Source attribution of the light absorbing aerosols was done using a positive matrix factorization (PMF) model. Four sources were found for each data set (crop and grass burning, boreal biomass burning, pollution and marine). For both data sets, the crops and grass biomass burning was the main source of both LAA species, suggesting the non-BC LAA was brown carbon. Depth profiles at most of the sites allowed assessment of the seasonal variation in the source strengths. The biomass burning sources dominated in the spring but pollution played a more significant (though rarely dominant) role in the fall, winter and, for Greenland, summer. The PMF analysis is consistent with trajectory analysis and satellite fire maps

    First-Line Trastuzumab Plus an Aromatase Inhibitor, With or Without Pertuzumab, in Human Epidermal Growth Factor Receptor 2-Positive and Hormone Receptor-Positive Metastatic or Locally Advanced Breast Cancer (PERTAIN): A Randomized, Open-Label Phase II Trial

    Get PDF
    To assess pertuzumab plus trastuzumab and an aromatase inhibitor (AI) in patients with human epidermal growth factor receptor 2 (HER2)-positive and hormone receptor-positive metastatic/locally advanced breast cancer (MBC/LABC)

    Clear-Column Radiative Closure During ACE-Asia: Comparison of Multiwavelength Extinction Derived from Particle Size and Composition with Results from Sun Photometry

    Get PDF
    From March to May 2001, aerosol size distributions and chemical compositions were measured using differential mobility analyzers (DMA), an aerodynamic particle sizer (APS), Micro-Orifice Uniform Deposit Impactors (MOUDI), and denuder samplers onboard the Twin Otter aircraft as part of the Aerosol Characterization Experiment (ACE)-Asia campaign. Of the 19 research flights, measurements on four flights that represented different aerosol characteristics are analyzed in detail. Clear-column radiative closure is studied by comparing aerosol extinctions predicted using in situ aerosol size distribution and chemical composition measurements to those derived from the 14-wavelength NASA Ames Airborne Tracking Sun photometer (AATS-14). In the boundary layer, pollution layers, and free troposphere with no significant mineral dust present, aerosol extinction closure was achieved within the estimated uncertainties over the full range of wavelengths of AATS-14. Aerosol extinctions predicted based on measured size distributions also reproduce the wavelength dependence derived from AATS-14 data. Considering all four flights, the best fit lines yield Predicted/Observed ratios in boundary and pollution layers of 0.97 ± 0.24 and 1.07 ± 0.08 at λ = 525 nm and 0.96 ± 0.21 and 1.08 ± 0.08 at λ = 1059 nm, respectively. In free troposphere dust layers, aerosol extinctions predicted from the measured size distributions were generally smaller than those derived from the AATS-14 data, with Predicted/Observed ratios of 0.65 ± 0.06 and 0.66 ± 0.05 at 525 and 1059 nm, respectively. A detailed analysis suggests that the discrepancy is likely a result of the lack of the knowledge of mineral dust shape as well as variations in aerosol extinction derived from AATS-14 data when viewing through horizontally inhomogeneous layers

    Clear-column radiative closure during ACE-Asia: Comparison of multiwavelength extinction derived from particle size and composition with results from Sun photometry

    Get PDF
    From March to May 2001, aerosol size distributions and chemical compositions were measured using differential mobility analyzers (DMA), an aerodynamic particle sizer (APS), Micro-Orifice Uniform Deposit Impactors (MOUDI), and denuder samplers onboard the Twin Otter aircraft as part of the Aerosol Characterization Experiment (ACE)-Asia campaign. Of the 19 research flights, measurements on four flights that represented different aerosol characteristics are analyzed in detail. Clear-column radiative closure is studied by comparing aerosol extinctions predicted using in situ aerosol size distribution and chemical composition measurements to those derived from the 14-wavelength NASA Ames Airborne Tracking Sun photometer (AATS-14). In the boundary layer, pollution layers, and free troposphere with no significant mineral dust present, aerosol extinction closure was achieved within the estimated uncertainties over the full range of wavelengths of AATS-14. Aerosol extinctions predicted based on measured size distributions also reproduce the wavelength dependence derived from AATS-14 data. Considering all four flights, the best fit lines yield Predicted/Observed ratios in boundary and pollution layers of 0.97 ± 0.24 and 1.07 ± 0.08 at λ = 525 nm and 0.96 ± 0.21 and 1.08 ± 0.08 at λ = 1059 nm, respectively. In free troposphere dust layers, aerosol extinctions predicted from the measured size distributions were generally smaller than those derived from the AATS-14 data, with Predicted/Observed ratios of 0.65 ± 0.06 and 0.66 ± 0.05 at 525 and 1059 nm, respectively. A detailed analysis suggests that the discrepancy is likely a result of the lack of the knowledge of mineral dust shape as well as variations in aerosol extinction derived from AATS-14 data when viewing through horizontally inhomogeneous layers

    In situ aerosol-size distributions and clear-column radiative closure during ACE-2

    Get PDF
    As part of the second Aerosol Characterization Experiment (ACE-2) during June and July of 1997, aerosol-size distributions were measured on board the CIRPAS Pelican aircraft through the use of a DMA and 2 OPCs. During the campaign, the boundary-layer aerosol typically possessed characteristics representative of a background marine aerosol or a continentally influenced aerosol, while the free-tropospheric aerosol was characterized by the presence or absence of a Saharan dust layer. A range of radiative closure comparisons were made using the data obtained during vertical profiles flown on 4 missions. Of particular interest here are the comparisons made between the optical properties as determined through the use of measured aerosol-size distributions and those measured directly by an airborne 14-wavelength sunphotometer and 3 nephelometers. Variations in the relative humidity associated with each of the direct measurements required consideration of the hygroscopic properties of the aerosol for size-distribution-based calculations. Simultaneous comparison with such a wide range of directly-measured optical parameters not only offers evidence of the validity of the physicochemical description of the aerosol when closure is achieved, but also provides insight into potential sources of error when some or all of the comparisons result in disagreement. Agreement between the derived and directly-measured optical properties varied for different measurements and for different cases. Averaged over the 4 case studies, the derived extinction coefficient at 525 nm exceeded that measured by the sunphotometer by 2.5% in the clean boundary layer, but underestimated measurements by 13% during pollution events. For measurements within the free troposphere, the mean derived extinction coefficient was 3.3% and 17% less than that measured by the sunphotometer during dusty and non-dusty conditions, respectively. Likewise, averaged discrepancies between the derived and measured scattering coefficient were −9.6%, +4.7%, +17%, and −41% for measurements within the clean boundary layer, polluted boundary layer, free troposphere with a dust layer, and free troposphere without a dust layer, respectively. Each of these quantities, as well as the majority of the >100 individual comparisons from which they were averaged, were within estimated uncertainties

    Oxalic acid in clear and cloudy atmospheres: Analysis of data from International Consortium for Atmospheric Research on Transport and Transformation 2004

    Get PDF
    Oxalic acid is often the leading contributor to the total dicarboxylic acid mass in ambient organic aerosol particles. During the 2004 International Consortium for Atmospheric Research on Transport and Transformation (ICARTT) field campaign, nine inorganic ions (including SO_4^(2−)) and five organic acid ions (including oxalate) were measured on board the Center for Interdisciplinary Remotely Piloted Aircraft Studies (CIRPAS) Twin Otter research aircraft by a particle-into-liquid sampler (PILS) during flights over Ohio and surrounding areas. Five local atmospheric conditions were studied: (1) cloud-free air, (2) power plant plume in cloud-free air with precipitation from scattered clouds overhead, (3) power plant plume in cloud-free air, (4) power plant plume in cloud, and (5) clouds uninfluenced by local pollution sources. The aircraft sampled from two inlets: a counterflow virtual impactor (CVI) to isolate droplet residuals in clouds and a second inlet for sampling total aerosol. A strong correlation was observed between oxalate and SO_4^(2−) when sampling through both inlets in clouds. Predictions from a chemical cloud parcel model considering the aqueous-phase production of dicarboxylic acids and SO_4^(2−) show good agreement for the relative magnitude of SO_4^(2−) and oxalate growth for two scenarios: power plant plume in clouds and clouds uninfluenced by local pollution sources. The relative contributions of the two aqueous-phase routes responsible for oxalic acid formation were examined; the oxidation of glyoxylic acid was predicted to dominate over the decay of longer-chain dicarboxylic acids. Clear evidence is presented for aqueous-phase oxalic acid production as the primary mechanism for oxalic acid formation in ambient aerosols
    • …
    corecore